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Hydroxychloroquine Sulfate - 0591-0698-01 - (Hydroxychloroquine Sulfate)

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Drug Information of Hydroxychloroquine Sulfate

Product NDC: 0591-0698
Proprietary Name: Hydroxychloroquine Sulfate
Non Proprietary Name: Hydroxychloroquine Sulfate
Active Ingredient(s): 200    mg/1 & nbsp;   Hydroxychloroquine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxychloroquine Sulfate

Product NDC: 0591-0698
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040133
Marketing Category: ANDA
Start Marketing Date: 19951130

Package Information of Hydroxychloroquine Sulfate

Package NDC: 0591-0698-01
Package Description: 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0591-0698-01)

NDC Information of Hydroxychloroquine Sulfate

NDC Code 0591-0698-01
Proprietary Name Hydroxychloroquine Sulfate
Package Description 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0591-0698-01)
Product NDC 0591-0698
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine Sulfate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19951130
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name HYDROXYCHLOROQUINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Hydroxychloroquine Sulfate


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